Evidence map›Paper›PMID 38257286›Full record

ArticleMolecules (Basel, Switzerland)2024

Design, Synthesis, and Evaluation of New Hybrid Derivatives of 5,6-Dihydro-4

Anna A Skoptsova, Athina Geronikaki, Nadezhda P Novichikhina, Alexey V Sulimov, Ivan S Ilin, Vladimir B Sulimov, Georgii A Bykov, Nadezhda A Podoplelova, Oleg V Pyankov, Khidmet S Shikhaliev

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Anna A SkoptsovaDepartment of Organic Chemistry, Faculty of Chemistry, Voronezh State University, 1 Universitetskaya Sq., 394018 Voronezh, Russia.ORCID 0000-0002-9859-6476
Athina GeronikakiSchool of Pharmacy, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.ORCID 0000-0001-9894-7777
Nadezhda P NovichikhinaDepartment of Organic Chemistry, Faculty of Chemistry, Voronezh State University, 1 Universitetskaya Sq., 394018 Voronezh, Russia.ORCID 0000-0001-8167-6093
Alexey V SulimovResearch Computing Center, Lomonosov Moscow State University, 119992 Moscow, Russia.ORCID 0000-0002-8767-642X
Ivan S IlinResearch Computing Center, Lomonosov Moscow State University, 119992 Moscow, Russia.ORCID 0000-0002-3612-393X
Vladimir B SulimovResearch Computing Center, Lomonosov Moscow State University, 119992 Moscow, Russia.ORCID 0000-0002-7102-6107
Georgii A BykovDepartment of Biophysics at the Faculty of Physics, Lomonosov Moscow State University, 119992 Moscow, Russia.ORCID 0000-0002-5623-723X
Nadezhda A PodoplelovaCenter for Theoretical Problems of Physicochemical Pharmakology, 119991 Moscow, Russia.ORCID 0000-0001-8013-1112
Oleg V PyankovState Research Center of Virology and Biotechnology "Vector", 630559 Koltsovo, Russia.ORCID 0000-0003-3340-8750
Khidmet S ShikhalievDepartment of Organic Chemistry, Faculty of Chemistry, Voronezh State University, 1 Universitetskaya Sq., 394018 Voronezh, Russia.ORCID 0000-0002-6576-0305
Lomonosov Moscow State University · RUVoronezh State University · RUAristotle University of Thessaloniki · GRCenter for Theoretical Problems of Physicochemical Pharmacology · RUState Research Center of Virology and Biotechnology VECTOR · RU

Funding

Federal Service for Supervision of Consumer Protection GZ 43/21
6 · The paper itself

Abstract

Cardiovascular diseases caused by blood coagulation system disorders are one of the leading causes of morbidity and mortality in the world. Research shows that blood clotting factors are involved in these thrombotic processes. Among them, factor Xa occupies a key position in the blood coagulation cascade. Another coagulation factor, XIa, is also a promising target because its inhibition can suppress thrombosis with a limited contribution to normal hemostasis. In this regard, the development of dual inhibitors as new generation anticoagulants is an urgent problem. Here we report the synthesis and evaluation of novel potential dual inhibitors of coagulation factors Xa and XIa. Based on the principles of molecular design, we selected a series of compounds that combine in their structure fragments of pyrrolo[3,2,1-

Indexed as

Cardiovascular DiseasesFactor XaAnticoagulantsBlood CoagulationHumansThrombinAnticoagulantsFactor XaThrombin5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-2-oneanticoagulant activityblood coagulationdual activityfactor Xafactor XIainhibitormolecular dockingthiazolethrombin

Identifiers

PMID38257286
PMCPMC10818416
OpenAlexW4390740290

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.